CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 200 enrolled
Drug / intervention
XIENCE V® Everolimus Eluting Coronary Stent System +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00531011
NCT00531011Phase 4Completed

EXecutive Randomized Controlled Trial (RCT): XIENCE V® Everolimus Eluting Coronary Stent System (XIENCE V® EECSS) in the Treatment of the Specific Setting of Patients With Multi-vessel Coronary Artery Disease.

Abbott Medical Devices·interventional·Posted Sep 18, 2007·Updated Jun 8, 2015

In Brief

A Phase 4 clinical trial evaluating XIENCE V® Everolimus Eluting Coronary Stent System and TAXUS® Liberté™ Paclitaxel Eluting Coronary Stent System for Coronary Disease and 3 related conditions. Completed, enrolled 200 participants across 24 sites.

Detailed Summary

The purpose of this two part study is the assessment of the performance of the XIENCE V® Everolimus Eluting Coronary Stent System (XIENCE V® EECSS) in the treatment of the specific setting of patients with Multi-Vessel Coronary Artery Disease (MVD).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesItaly
Collaborators--

Timeline

Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 18, 2007
Enrollment StartSep 1, 2007
Primary CompletionMar 1, 2010
Study CompletionJun 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 18.8 years ago

Interventions

XIENCE V® Everolimus Eluting Coronary Stent Systemdevice

Coronary artery placement of a drug-eluting stent

TAXUS® Liberté™ Paclitaxel Eluting Coronary Stent Systemdevice

Coronary artery placement of a drug-eluting stent